US7241889B2

US7241889B2 - 6-formyl-tetrahydropteridines, process for their manufacture and use thereof as medicaments

Info

Publication number: US7241889B2
Application number: US11/179,234
Authority: US
Inventors: Matthias Hoffmann; Matthias Grauert; Martin Steegmaier; Flavio Solca
Original assignee: Boehringer Ingelheim International GmbH
Current assignee: Boehringer Ingelheim International GmbH
Priority date: 2004-07-16
Filing date: 2005-07-12
Publication date: 2007-07-10
Also published as: WO2006008028A1; JP2008506644A; WO2006008028A8; DE102004034623A1; CA2573943A1; CA2573943C; EP1776363A1; EP1776363B1; JP2012140455A; JP5009155B2; US20060014751A1

Abstract

Disclosed are 6-formyl-tetrahydropteridines of the formula (I)

wherein the groups R¹to R⁶have the meanings given in the claims and specification, the isomers thereof, methods of preparing these 6-formyl-tetrahydropteridines and their use as medicaments.

Description

APPLICATION DATA

This application claims benefit to German application DE 10 2004 034 623.2 filed Jul. 16, 2004.

The present invention relates to new 6-formyl-tetrahydropteridines of general formula (I)

wherein the groups R¹to R⁶have the meanings given in the claims and specification, the isomers thereof, processes for preparing these 6-formyl-tetrahydropteridines and their use as medicaments.

BACKGROUND TO THE INVENTION

Pteridinone derivatives are known from the prior art as active substances with an antiproliferative activity. WO 01/019825 and WO 03/020722 describe the use of pteridinone derivatives for the treatment of tumoral diseases.

Tumour cells wholly or partly elude regulation and control by the body and are characterised by uncontrolled growth. This is based on the one hand on the loss of control proteins, such as e.g. Rb, p16, p21 and p53 and also on the activation of so-called accelerators of the cell cycle, the cyclin-dependent kinases (CDK's).

In addition, the protein kinase Aurora B has been described as having an essential function during entry into mitosis. Aurora B phosphorylates histone H3 at Ser10 and thus initiates chromosome condensation (Hsu et al. 2000, Cell 102:279-91). A specific cell cycle arrest in the G2/M phase may however also be triggered e.g. by the inhibition of specific phosphatases such as e.g. Cdc25C (Russell and Nurse 1986, Cell 45:145-53). Yeasts with a defective Cdc25 gene arrest in the G2 phase, while overexpression of Cdc25 leads to premature entry into the mitosis phase (Russell and Nurse 1987, Cell 49:559-67). Moreover, an arrest in the G2/M phase may also be triggered by the inhibition of certain motor proteins, the so-called kinesins such as e.g. Eg5 (Mayer et al. 1999, Science 286:971-4), or by agents which stabilise or destabilise microtubules (e.g. colchicin, taxol, etoposide, vinblastin, vincristine) (Schiff and Horwitz 1980, Proc Natl Acad Sci USA 77:1561-5).

In addition to the cyclin-dependent and Aurora kinases the so-called polo-like kinases, a small family of serine/threonine kinases, play an important part in the regulation of the eukaryotic cell cycle. Hitherto, the polo-like kinases PLK-1, PLK-2, PLK-3 and PLK-4 have been described in the literature. PLK-1 in particular has been shown to play a central part in the regulation of the mitosis phase. PLK-1 is responsible for the maturation of the centrosomes, for the activation of phosphatase Cdc25C, and for the activation of the Anaphase Promoting Complex (Glover et al. 1998, Genes Dev. 12:3777-87; Qian et al. 2001, Mol Biol Cell. 12:1791-9). The injection of PLK-1 antibodies leads to a G2 arrest in untransformed cells, whereas tumour cells arrest in the mitosis phase (Lane and Nigg 1996, J. Cell Biol. 135:1701-13). Overexpression of PLK-1 has been demonstrated for various types of tumour, such as non-small-cell lung cancer, plate epithelial carcinoma, breast and colorectal carcinoma (Wolf et al. 1997, Oncogene 14 :543-549; Knecht et al. 1999, Cancer Res. 59:2794-2797; Wolf et al. 2000, Pathol. Res. Pract. 196:753-759; Takahashi et al. 2003, Cancer Sci. 94:148-52). Therefore, this category of proteins also constitutes an interesting approach to therapeutic intervention in proliferative diseases (Liu and Erikson 2003, Proc Natl Acad Sci USA 100:5789-5794).

The resistance of many types of tumours calls for the development of new pharmaceutical compositions for combating tumours.

The aim of the present invention is to provide new compounds having an antiproliferative activity.

DETAILED DESCRIPTION OF THE INVENTION

Surprisingly it has been found that compounds of general formula (I) wherein the groups R¹to R⁶have the meanings given hereinafter act as inhibitors of specific cell cycle kinases particularly the polo-like kinases. The compounds named have an antiproliferative activity, in that they arrest cells in the mitosis phase of the cell cycle before programmed cell death is initiated in the arrested cells. Thus, the compounds according to the invention may be used for example to treat diseases connected with the activity of specific cell cycle kinases and characterised by excessive or abnormal cell proliferation.

The present invention therefore relates to compounds of general formula (I)

wherein

R¹, R²which may be identical or different denote a group selected from among optionally substituted C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, aryl, heteroaryl, C₃-C₈-cycloalkyl, C₃-C₈-heterocycloalkyl, —X-aryl, —X-heteroaryl, —X-cycloalkyl, —X-heterocycloalkyl, —NR⁷-aryl, —NR⁷-heteroaryl, —NR⁷-cycloalkyl and —NR⁷-heterocycloalkyl,
or
a group selected from among hydrogen, halogen, COXR⁷, CON(R⁷)₂, COR⁷and XR⁷,
or
R¹and R²together denote a 2- to 5-membered alkyl bridge which may contain 1 to 2 heteroatoms,
R³denotes hydrogen or a group selected from among optionally substituted C₁-C₁₂-alkyl, C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl, aryl, heteroaryl, —C₃-C₁₂-cycloalkyl, C₃-C₁₂-cycloalkenyl, C₇-C₁₂-polycycloalkyl, C₇-C₁₂-polycycloalkenyl and C₅-C₁₂-spirocycloalkyl or
R¹and R³or R²and R³together denote a saturated or unsaturated C₃-C₄-alkyl bridge which may contain 1 to 2 heteroatoms,
R⁴denotes optionally substituted aryl, benzyl or heteroaryl,
R⁵denotes hydrogen, —CO—NH—C₁-C₄-alkyl, —CO—C₁-C₄-alkyl or —CO—X—C₁-C₄-alkyl,
R⁶denotes a group selected from among hydrogen, NH₂, XH, halogen and einer optionally by one or more halogen atoms substituted C₁-C₃-alkyl group,
R⁷each independently of one another denote hydrogen or a group selected from among optionally substituted C₁-C₄-alkyl, C₂-C₄-alkenyl, C₂-C₄-alkynyl, benzyl and phenyl,
and
X denotes O or S,
optionally in the form of the tautomers, racemates, enantiomers, diastereomers and mixtures thereof, and optionally the pharmacologically acceptable acid addition salts, solvates or hydrates thereof.

Preferred are compounds of formula (I), wherein

R¹to R⁴and R⁷are as hereinbefore defined and
R⁵and R⁶denote hydrogen.

Also preferred are compounds of formula (I), wherein

R³to R⁷are as hereinbefore defined and
R¹, R²which may be identical or different denote hydrogen or a group selected from among optionally substituted C₁-C₆-alkyl, C₂-C₆-alkenyl, and C₂-C₆-alkynyl,
or
R¹and R²together denote a 2- to 5-membered alkyl bridge.

Also preferred are compounds of formula (I), wherein

R¹, R²and R⁴to R⁷are as hereinbefore defined,
and
R³is hydrogen or a group selected from among optionally substituted C₁-C₁₂-alkyl, C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl and C₆-C₁₄-aryl, or
a group selected from among optionally substituted C₃-C₁₂-cycloalkyl, C₃-C₁₂-cycloalkenyl, C₇-C₁₂-polycycloalkyl, C₇-C₁₂-polycycloalkenyl and C₅-C₁₂-spirocycloalkyl.

Particularly preferred are compounds of formula (I), wherein

R¹to R³and R⁵to R⁷are as hereinbefore defined,
and
R⁴denotes a group of general formula

R⁸which may be identical or different denote hydrogen or a group selected from among optionally substituted C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —O—C₁-C₆-alkyl, —O—C₂-C₆-alkenyl, —O—C₂-C₆-alkynyl, heterocycloalkyl, C₃-C₆-cycloalkyl, aryl, heteroaryl, —O-aryl, —O-heteroaryl, —O-cycloalkyl, and —O-heterocycloalkyl or
a group selected from among hydrogen, —CONH₂, —COOR⁷, —OCON(R⁷)₂, —N(R⁷)₂, —NHCOR⁷, —NHCON(R⁷)₂, —NO₂, CF₃, halogen, —O—C₁-C₆-alkyl-Q¹, —CONR⁷—C₁-C₁₀-alkyl-Q¹, —CONR⁷—C₁-C₁₀-alkenyl-Q¹, —CONR⁷—Q², halogen, OH, —SO₂R⁷, —SO₂N(R⁷)₂, —COR⁷, —COOR⁷, —N(R⁷)₂, —NHCOR⁷, —CONR⁷OC₁-C₁₀-alkyl-Q¹and CONR⁷O—Q²,
or
adjacent R⁸groups together denote a bridge of general formula a), b), c) or d),

Y denotes O, S or NR¹¹,
m denotes 0, 1 or 2
R⁹denotes C₁-C₆-alkyl
R¹⁰denotes hydrogen or a group selected from among optionally substituted phenyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, —C₁-C₃-alkyl-phenyl, —C₁-C₃-alkyl-pyridyl, —C₁-C₃-alkyl-pyrazinyl, —C₁-C₃-alkyl-pyrimidinyl and —C₁-C₃-alkyl-pyridazinyl, piperidinyl, piperazinyl,
R¹¹denotes hydrogen or C¹-C⁴-alkyl
Q¹denotes hydrogen, —NHCOR⁷, or a group selected from among an optionally substituted —NH-aryl, —NH-heteroaryl, aryl, heteroaryl, C₃-C₈-cycloalkyl and heterocycloalkyl group,
Q²denotes hydrogen or a group selected from among an optionally substituted aryl, heteroaryl, C₃-C₈-heterocycloalkyl-, C₃-C₈-cycloalkyl- and C₁-C₄-alkyl-C₃-C₈-cycloalkyl group,
and
n denotes 0, 1, 2, 3, 4 or 5.

Particularly preferred are compounds of formula (I), wherein

Q¹, Q², n, R⁴to R⁸are as hereinbefore defined,
R¹, R²which may be identical or different denote hydrogen or a group selected from among methyl, ethyl, propyl, allyl and propargyl
or
R¹and R²together denote cyclopropyl,
R³is hydrogen, or denotes optionally substituted C₁-C₆-alkyl or optionally substituted C₃-C₁₂-cycloalkyl.

Most preferred are compounds of formula (I), wherein

Q¹, Q², n, R¹to R⁴, R⁶to R⁷have the meanings specified,
and
R⁸which may be identical or different denote hydrogen or a group selected from among halogen, (C₁-C₂-alkyl)₂N, CF₃, NH₂SO₂, —CONH—C₆-C₁₄-aryl, —CONH—C₁-C₄-alkyl-C₆-C₁₄-aryl and —O—C₁-C₄-alkyl, CONH—C₃-C₈-cycloalkyl-heterocycloalkyl.

The invention further relates to compounds of formula (I) for use as pharmaceutical compositions.

Of particular importance according to the invention are compounds of formula (I) for use as pharmaceutical compositions with an antiproliferative activity.

The invention also relates to the use of a compound of formula (I) for preparing a pharmaceutical composition for the treatment and/or prevention of diseases selected from among cancer, bacterial and viral infections, inflammatory and autoimmune diseases, chemotherapy-induced alopecia and mucositis, cardiovascular diseases, nephrological diseases, as well as chronic and acute neurodegenerative diseases, preferably for the treatment of cancer, inflammatory and autoimmune diseases, particularly preferably for the treatment of cancer and inflammatory diseases.

The invention further relates to the use of a compound of formula (I) for preparing a pharmaceutical composition for inhibiting the polo-like kinases, particularly the polo-like kinase PLK-1.

The invention further relates to the use of a compound of formula (I) for preparing a pharmaceutical composition for the treatment and/or prevention of tumour diseases based on the overexpression of the polo-like kinases, particularly the PLK-1 kinases.

The invention further relates to a method for the treatment and/or prevention of diseases selected from among cancer, bacterial and viral infections, inflammatory and autoimmune diseases, chemotherapy-induced alopecia and mucositis, cardiovascular diseases, nephrological diseases, as well as chronic and acute neurodegenerative diseases, preferably for the treatment of cancer, inflammatory and autoimmune diseases, particularly preferably for the treatment of cancer and inflammatory diseases, in which an effective amount of a compound of formula (I) is administered to a patient.

The invention also relates to pharmaceutical preparations, containing as active substance one or more compounds of general formula (I) optionally combined with conventional excipients and/or carriers.

The term alkyl groups, including alkyl groups which are a part of other groups, denotes branched and unbranched alkyl groups with 1 to 12 carbon atoms, preferably 1-6, most preferably 1-4 carbon atoms, such as, for example: methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl and decyl. Unless otherwise stated, the abovementioned terms propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl and decyl include all the possible isomeric forms. For example, the term propyl includes the two isomeric groups n-propyl and iso-propyl, the term butyl includes n-butyl, iso-butyl, sec. butyl and tert.-butyl, the term pentyl includes iso-pentyl, neopentyl, etc.

In the abovementioned alkyl groups one or more hydrogen atoms may optionally be replaced by other groups. For example these alkyl groups may be substituted by methyl, chlorine or fluorine, preferably fluorine. All the hydrogen atoms of the alkyl group may optionally also be replaced.

The term alkyl bridge, unless otherwise stated, denotes branched and unbranched alkyl groups with 2 to 5 carbon atoms, for example ethylene, propylene, isopropylene, n-butylene, iso-butyl, sec. butyl and tert.-butyl etc. bridges. Ethylene, propylene and butylene bridges are particularly preferred. In the alkyl bridges mentioned 1 to 2 C-atoms may optionally be replaced by one or more heteroatoms selected from among oxygen, nitrogen or sulphur.

The term alkenyl groups (including those which are a part of other groups) denotes branched and unbranched alkylene groups with 2 to 10 carbon atoms, preferably 2 to 6 carbon atoms, most preferably 2-3 carbon atoms, provided that they have at least one double bond. Examples include: ethenyl, propenyl, butenyl, pentenyl etc. Unless otherwise stated, the abovementioned terms propenyl, butenyl, etc also include all the possible isomeric forms. For example, the term butenyl includes 1-butenyl, 2-butenyl, 1-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-1-propenyl, 2-methyl-2-propenyl and 1-ethyl-1-ethenyl.

In the abovementioned alkenyl groups, unless otherwise stated, one or more hydrogen atoms may optionally be replaced by other groups. For example, these alkenyl groups may be substituted by methyl, chlorine or fluorine, preferably fluorine. All the hydrogen atoms of the alkenyl group may optionally also be replaced.

The term alkynyl groups (including those which are a part of other groups) denotes branched and unbranched alkynyl groups with 2 to 10 carbon atoms, provided that they have at least one triple bond, for example ethynyl, propargyl, butynyl, pentynyl, hexynyl etc., preferably ethynyl or propynyl.

In the abovementioned alkynyl groups, unless otherwise stated, one or more hydrogen atoms may optionally be replaced by other groups. For example, these alkynyl groups may be substituted by methyl, chlorine or fluorine, preferably fluorine. All the hydrogen atoms of the alkynyl group may optionally also be replaced.

The term aryl denotes an aromatic ring system with 6 to 14 carbon atoms, preferably 6 or 10 carbon atoms, preferably phenyl, which, unless otherwise stated, may carry one or more of the following substituents, for example: OH, NO₂, CN, OMe, —OCHF₂, —OCF₃, —NH₂, halogen, preferably fluorine or chlorine, C₁-C₁₀-alkyl, preferably C₁-C₅-alkyl, preferably C₁-C₃-alkyl, particularly preferably methyl or ethyl, —O—C₁-C₃-alkyl, preferably —O-methyl or —O-ethyl, —COOH, —COO—C₁-C₄-alkyl, preferably —O-methyl or —O-ethyl, or —CONH₂.

As heteroaryl groups wherein up to two C atoms are replaced by one or two nitrogen atoms may be mentioned, for example, pyrrole, pyrazole, imidazole, triazole, pyridine, pyrimidine, while each of the above-mentioned heteroaryl rings may optionally also be anellated to a benzene ring, preferably benzimidazole, and these heterocycles, unless stated to the contrary, may for example carry one or more of the following substituents: F, Cl, Br, OH, OMe, methyl, ethyl, CN, CONH₂, NH₂, optionally substituted phenyl, optionally substituted heteroaryl, preferably optionally substituted pyridyl.

Examples of cycloalkyl groups are cycloalkyl groups with 3-12 carbon atoms, preferably 3-8 carbon atoms, for example cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl, preferably cyclopropyl, cyclopentyl or cyclohexyl, while each of the above-mentioned cycloalkyl groups may optionally be bridged and/or may also carry one or more substituents, for example: OH, NO₂, CN, OMe, —OCHF₂, —OCF₃, —NH₂or halogen, preferably fluorine or chlorine, C₁-C₁₀-alkyl, preferably C₁-C₅-alkyl, preferably C₁-C₃-alkyl, particularly preferably methyl or ethyl, —O—C₁-C₃-alkyl, preferably —O-methyl or —O-ethyl, —COOH, —COO—C₁-C₄-alkyl, preferably —COO-methyl or —COO-ethyl or —CONH₂. Particularly preferred substituents of the cycloalkyl groups are ═O, OH, NH₂, methyl or F.

Examples of cycloalkenyl groups are cycloalkyl groups with 3-12 carbon atoms which have at least one double bond, for example cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl or cycloheptenyl, preferably cyclopropenyl, cyclopententyl or cyclohexenyl, while each of the above-mentioned cycloalkenyl groups may optionally be bridged and/or may also carry one or more substituents.

“═O” denotes an oxygen atom linked by a double bond.

Examples of heterocycloalkyl groups, unless otherwise stated in the definitions, are 3 to 12 membered, preferably 5-, 6- or 7-membered, saturated or unsaturated heterocycles, which may contain as heteroatoms nitrogen, oxygen or sulphur, for example tetrahydrofuran, tetrahydrofuranone, γ-butyrolactone, α-pyran, γ-pyran, dioxolane, tetrahydropyran, dioxane, dihydrothiophene, thiolane, dithiolane, pyrroline, pyrrolidine, pyrazoline, pyrazolidine, imidazoline, imidazolidine, tetrazole, piperidine, pyridazine, pyrimidine, pyrazine, piperazine, triazine, tetrazine, morpholine, thiomorpholine, diazepan, oxazine, tetrahydro-oxazinyl, isothiazole, pyrazolidine, preferably morpholine, pyrrolidine, piperidine or piperazine, while the heterocyclic group may optionally be bridged and/or may also carry substituents, for example C₁-C₄-alkyl, preferably methyl, ethyl or propyl.

Examples of polycycloalkyl groups are optionally substituted, bi-, tri-, tetra- or pentacyclic cycloalkyl groups, for example pinane, 2.2.2-octane, 2.2.1-heptane or adamantane. Examples of polycycloalkenyl groups are optionally bridged and/or substituted, 8-membered bi-, tri-, tetra- or pentacyclic cycloalkenyl groups, preferably bicycloalkenyl or tricycloalkenyl groups, if they contain at least one double bond, for example norbornene.

Examples of spiroalkyl groups are optionally substituted spirocyclic C₅-C₁₂alkyl groups.

The term halogen generally denotes fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine, particularly preferably chlorine.

The compounds according to the invention may be present in the form of the individual optical isomers, mixtures of the individual enantiomers, diastereomers or racemates, in the form of the tautomers, in the form of the solvates, preferably in the form of the hydrates thereof and also in the form of the free bases or the corresponding acid addition salts with pharmacologically acceptable acids—such as for example acid addition salts with hydrohalic acids, for example hydrochloric or hydrobromic acid, or organic acids, such as for example oxalic, fumaric, diglycolic or methanesulphonic acid.

The substituent R¹may represent a group selected from among optionally substituted C₁-C₁₀-alkyl, preferably C₁-C₄-alkyl, particularly preferably methyl, ethyl or propyl, C₂-C₁₀-alkenyl, preferably allyl, C₂-C₁₀-alkynyl, preferably propargyl, aryl, preferably phenyl, heteroaryl, C₃-C₈-cycloalkyl, C₃-C₈-heterocycloalkyl, —X-aryl, —X-heteroaryl, —X-cycloalkyl, —X-heterocycloalkyl, —NR⁷-aryl, —NR⁷-heteroaryl, —NR⁷-cycloalkyl and —NR⁷-heterocycloalkyl,

or

a group selected from among hydrogen, halogen, COXR⁷, CON(R⁷)₂, COR⁷and XR⁷.

Preferably the substituent R¹denotes ethyl or hydrogen, particularly preferably hydrogen.

The substituent R²may represent a group selected from among optionally substituted C₁-C₁₀-alkyl, preferably C₁-C₄-alkyl, particularly preferably methyl, ethyl or propyl, C₂-C₁₀-alkenyl, preferably allyl, C₂-C₁₀-alkynyl, preferably propargyl, aryl, preferably phenyl, heteroaryl, C₃-C₈-cycloalkyl, C₃-C₈-heterocycloalkyl, —X-aryl, —X-heteroaryl, —X-cycloalkyl, —X-heterocycloalkyl, —NR⁷-aryl, —NR⁷-heteroaryl, —NR⁷-cycloalkyl and —NR⁷-heterocycloalkyl,

or

Preferably the substituent R²denotes methyl, ethyl, allyl, propargyl or hydrogen, particularly preferably methyl or ethyl.

The substituents R¹and R²may together denote a 2- to 5-membered alkyl bridge, preferably a 2-membered alkyl bridge which may contain 1 to 2 heteroatoms, for example oxygen, sulphur or nitrogen, preferably oxygen or nitrogen.

The substituent R³may represent hydrogen or a group selected from among optionally substituted C₁-C₁₂-alkyl, preferably C₂-C₆-alkyl, particularly preferably pentyl, C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl, aryl, heteroaryl, C₃-C₁₂-cycloalkyl, C₃-C₁₂-cycloalkenyl, C₇-C₁₂-polycycloalkyl, C₇-C₁₂-polycycloalkenyl and C₅-C₁₂-spirocycloalkyl or

R¹and R³or R²and R³together denote a saturated or unsaturated C₃-C₄-alkyl bridge which may contain 1 to 2 heteroatoms.

Preferably the substituent R₃denotes C₁-C₆-alkyl or —C₃-C₁₂-cycloalkyl, particularly preferably pentyl or cyclopentyl.

The substituent R⁴may optionally represent substituted aryl, benzyl or heteroaryl, preferably a group of general formula

The index n may represent 0, 1, 2, 3, 4 or 5, preferably 1 or 2, particularly preferably 1.

The substituent R⁵may represent a group selected from among hydrogen, —CO—NH—C₁-C₄-alkyl, —CO—C₁-C₄-alkyl or —CO—X—C₁-C₄-alkyl. Preferably the substituent R⁵denotes hydrogen.

The substituent R⁶may represent a group selected from among hydrogen, NH₂, XH, halogen and a C₁-C₃-alkyl group optionally substituted by one or more halogen atoms.

Preferably the substituent R⁶denotes hydrogen.

The substituent R⁷may each independently of one another denote hydrogen or a group selected from among optionally substituted C₁-C₄-alkyl, preferably methyl or ethyl, C₂-C₄-alkenyl, C₂-C₄-alkynyl, benzyl and phenyl. Preferably the substituent R⁷denotes hydrogen.

X may in each case independently of one another represent oxygen or sulphur, preferably oxygen.

The substituent R⁸which may be identical or different may denote hydrogen or a group selected from among optionally substituted C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —O—C₁-C₆-alkyl, —O—C₂-C₆-alkenyl, —O—C₂-C₆-alkynyl, heterocycloalkyl, C₃-C₆-cycloalkyl, aryl, heteroaryl, —O-aryl, —O-heteroaryl, —O-cycloalkyl, and —O-heterocycloalkyl or

a group selected from among hydrogen, —CONH₂, —COOR⁷, —OCON(R⁷)₂, —N(R⁷)₂, —NHCOR⁷—NHCON(R⁷)₂, —NO₂, CF₃, halogen, —O—C₁-C₆-alkyl-Q¹, —CONR⁷-C₁-C₁₀-alkyl-Q¹, —CONR⁷—C₁-C₁₀-alkenyl-Q¹, —CONR⁷-Q², halogen, OH, —SO₂R⁷, —SO₂N(R⁷)₂, —COR⁷, —COOR⁷, —N(R⁷)₂, —NHCOR⁷, —CONR⁷OC₁-C₁₀-alkyl-Q¹and CONR⁷O—Q²,
or
adjacent groups R⁸together denote a bridge of general formula a), b), c) or d),

Preferably the substituent R⁸denotes aryl, preferably phenyl, heteroaryl, particularly preferably pyridyl or pyrimidinyl, or a group selected from among —CONR⁷—Q², preferably —CONH—Q², —CONR⁷—C₁-C₁₀-alkyl-Q¹, preferably —CONH—C_1-2—Q, or —CONH—C₂—Q¹, CONR⁷—C₃-C₈-cycloalkyl-Q¹, preferably —CONH-cyclohexyl-Q¹or —CONH-cyclopentyl-Q¹

Y may represent O, S or NR¹¹, preferably NR¹¹.

m denotes 0, 1 or 2, preferably 1.

The substituent R⁹may represent C₁-C₆-alkyl, preferably methyl.

The substituent R¹⁰may represent hydrogen or a group selected from among optionally substituted phenyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, piperidinyl, piperazinyl, —C₁-C₃-alkyl-phenyl, —C₁-C₃-alkyl-pyridyl, —C₁-C₃-alkyl-pyrazinyl, —C₁-C₃-alkyl-pyrimidinyl and —C₁-C₃-alkyl-pyridazinyl.

Particularly preferably R¹⁰denotes pyridyl, pyrimidinyl, piperidinyl, piperazinyl.

The substituent R¹¹may represent hydrogen or C¹-C⁴-alkyl, preferably hydrogen or methyl.

Q¹may represent hydrogen, —NHCOR⁷, or a group selected from among an optionally substituted —NH-aryl, —NH-heteroaryl, aryl, preferably phenyl, heteroaryl, C₃-C₈-cycloalkyl and heterocycloalkyl group.

Particularly preferably Q¹denotes heteroaryl or heterocycloalkyl, particularly preferably pyridinyl, pyrimidinyl, morpholinyl, piperazinyl or piperidinyl, Q²denotes hydrogen or a group selected from among an optionally substituted aryl, preferably phenyl, heteroaryl, C₃-C₈-heterocycloalkyl-, C₃-C₈-cycloalkyl and C₁-C₄-alkyl-C₃-C₈-cycloalkyl group.

m may represent 0, 1, 2, 3, 4 or 5, preferably 1.

The compounds of general formula (I) may be prepared by the following method of synthesis, wherein the substituents of general formulae (A1) to (A4) and (I) have the above-mentioned meanings.

This method is to be understood as illustrating the invention without restricting it to the object thereof.

A compound of formula (A1) is reduced to the compound of formula (A2) which then forms 2-chloro-6-formyl-tetrahydropteridine (A3) with formic acid. Then compounds of general formula (A3) are reacted with a substituted amine to produce general formula (I), which may optionally undergo further transformations. Compounds of formula (A1) may be obtained according to WO 2003020722. 4-amino-N-cyclopropyl benzamide may be prepared for example according to the following literature: B. W. Horrem and T. E. Lynes, J. Med. Chem. 1963, 6, 528-532. trans-4-morpholino-cyclohexylamine 10 was prepared by the following methods:

Dibenzyl-4-morpholino-cyclohexylamine

3.9 g (30 mmol)) 4-dibenzylcyclohexanone were dissolved in 100 mL CH₂Cl₂and stirred with 3.9 g (45 mmol) morpholine and 9.5 g (45 mmol) of NaBH(OAc)₃for 12 hours at 25° C. Then the mixture was combined with water and potassium carbonate, the organic phase was separated off, dried and evaporated down. The residue was purified through a silica gel column (eluant: ethyl acetate 90/methanol 10+1% conc. ammonia). The appropriate fractions were evaporated down in vacuo.

Yield: 6.6 g (60%) cis-isomer and 2 g (18%) trans-isomer.

Alternatively, trans-dibenzyl-4-morpholino-cyclohexylamine may be prepared by the following method:

33 g (112 mmol) 4-dibenzylcyclohexanone were dissolved in 300 mL methanol, combined with 17.4 g (250 mmol) hydroxylamine hydrochloride and stirred for 4 hours at 60° C. The solvent was evaporated down in vacuo, combined with 500 mL water and 50 g potassium carbonate and extracted twice with 300 mL dichloromethane. The organic phases were dried, evaporated down in vacuo, the residue was crystallised from petroleum ether, dissolved in 1.5 L ethanol and heated to 70° C. 166 g of sodium was added batchwise and refluxed until the sodium dissolved. The solvent was removed, the residue was combined with 100 mL water and extracted twice with 400 mL ether. The organic phases were washed with water, dried, evaporated down in vacuo and the trans-isomer was isolated through a column (eluant: ethyl acetate 80/methanol 20+2% conc. ammonia).

Yield: 12.6 g (41%).

6.8 g (23 mmol) trans-1-amino-4-dibenzylaminocyclohexane was dissolved in 90 mL DMF and stirred with 5 mL (42 mmol) 2,2′-dichloroethylether and 5 g potassium carbonate for 8 hours at 100° C. After cooling, 30 mL water was added, the precipitated crystals were suction filtered and purified through a short column (eluant: ethyl acetate). The residue was crystallised from methanol and conc. hydrochloric acid as the dihydrochloride.

Yield: 7.3 g (72%).

General Procedures:

Step 1

In Step 1, 1 equivalent of compound (A1) and 1 to 5 equivalents, preferably 3-4 equivalents of sodium borohydride were stirred with boron trifluoride etherate in a diluent such as tetrahydrofuran, diethyl ether or dioxane, preferably tetrahydrofuran, for 12-24 h at 15-40° C.

To isolate the product the reaction mixture is then combined with water and hydrochloric acid and the organic solvent is eliminated in vacuo. The aqueous phase is then made basic with a base such as ammonia or sodium carbonate and extracted two to three times with an organic solvent such as, for example, diethyl ether or ethyl acetate, preferably ethyl acetate. The combined organic extracts are dried and the solvent is distilled off. The residue (compound A2) may be used in Step 2 without prior purification.

Step 2

The compound (A2) obtained in Step 1 is dissolved in formic acid and refluxed for 5 min to 1 h, preferably 15 minutes, to form the compound (A3). Then the formic acid is removed by distillation and the residue is recrystallised by the addition of one or more organic solvents, for example ethyl acetate, diethyl ether, dichloromethane, acetone, petroleum ether.

Step 3

- a) In Step 3, 1 equivalent of the 2-chloro-6-formyl-tetrahydropteridine (A3) is mixed with 1-3 equivalents of an amine and heated for 30 minutes to 4 h at 120° to 180° C., preferably 160° C. (see Diagram 2). After cooling the mixture is taken up in a suitable solvent and the product is crystallised or subjected to chromatographic purification.
- b) Alternatively, in Step 3, 1 equivalent of 2-chloro-6-formyl-tetrahydropteridine (A3) may also be stirred with 1-3 equivalents of an amine in an organic solvent such as dioxane or tetrahydrofuran, with 1 equivalent of an acid, for example p-toluenesulphonic acid, for 8 h to 48 h at reflux temperature. After cooling the mixture is taken up in a suitable solvent and the product is crystallised or subjected to chromatographic purification.

SYNTHESIS OF EXAMPLES 1 AND 5

In order to synthesise Examples 1 and 5 first of all an intermediate compound 2

is prepared as described hereinafter.
Synthesis of Intermediate Compound 2:

2 g of compound 1 are dissolved in 50 mL tetrahydrofuran and stirred with 1 g sodium borohydride and 3 mL boron trifluoride etherate at 25° C. for 18 h. Then 2 mL water and 20 mL 2N hydrochloric acid were added dropwise and the mixture was refluxed for 10 minutes. Then the tetrahydrofuran was separated off by distillation, the residue was combined with ammonia solution and the aqueous phase was extracted 2× with 50 mL ethyl acetate. The organic phase was washed with water, dried and evaporated down in vacuo. Any crystals precipitated were filtered off and washed with ether. 1.5 g of a compound 3 were obtained which was used for the next reaction without any further purification.

1.4 g of compound 3 were dissolved in 10 mL formic acid and refluxed for 15 minutes. Then the solution was evaporated down in vacuo and the residue was combined with ether, the precipitate was filtered off and washed with ether. This yielded 1.2 g of a product 4 which was used in the next step without any further purification.

1.2 g of compound 4 was stirred with 2.78 g ethyl 4-aminobenzoate without solvent for 2 h at 150° C. After cooling the reaction mixture was combined with 50 mL ethyl acetate, the precipitate formed was filtered off and washed with ether. This yielded 1.1 g of a product 5 which was used in the next step without any further purification.

1.1 g of compound 5 was dissolved in 10 mL methanol and 1 mL water and combined with 0.4 g sodium hydroxide, then the mixture was stirred for 24 h at 30° C. It was then evaporated down in vacuo, combined with 20 mL water and 0.8 mL acetic acid and extracted 2× with 50 mL methylene chloride. The organic phase was dried, evaporated down in vacuo and crystallised from acetone. 0.7 g of a solid 2 were obtained which was used for subsequent reactions.

EXAMPLE 1

0.1 g of 2 was stirred together with 0.5 g cyclopropylamine, 0.1 g of o-benzotriazolyl,N,N,N′, N′-tetramethyluronium tetrafluoroborate (TBTU), 0.5 mL N-ethyldiisopropylamine in 2 mL dimethylformamide for 30 minutes. Then 50 mL water and 1 g potassium carbonate was added and the mixture was extracted 2× with 50 mL dichloromethane. The organic phase was dried and evaporated down in vacuo. Then the mixture was fractionated by chromatography on silica gel, and the crude product thus obtained was dissolved in acetone, the solution was combined with ethereal HCl, evaporated down and crystallised from ether. 25 mg of a yellow powder were obtained.

EXAMPLE 5

0.1 g of 2 was stirred with 0.15 g of 3-aminopyridine, 0.1 g TBTU, 0.5 g N-ethyldiisopropylamine in 2 mL dimethylformamide for 2 h at 120° C. Then it was combined with 50 mL water and 1 g potassium carbonate and extracted twice with 50 mL methylene chloride. The organic phase was dried, the mixture was fractionated by chromatography on silica gel, the appropriate fractions were evaporated down in vacuo and the residue was crystallised from acetone. 10 mg of a yellow solid were obtained.

SYNTHESIS OF EXAMPLES 6 AND 8

In order to synthesise Examples 6 and 8 first of all an intermediate compound 7

is prepared as described below.
Synthesis of the Intermediate Compound 7:

4 g of compound 6 is dissolved in 100 mL tetrahydrofuran and stirred with 2 g sodium borohydride and 6 mL boron trifluoride etherate at 25° C. for 18 h. Then first 4 mL water then 40 mL 2N hydrochloric acid were slowly added dropwise to the suspension and the mixture was refluxed for 10 minutes. Then the tetrahydrofuran was separated off by distillation, the residue was combined with ammonia solution and the aqueous phase was extracted 2× with in each case 100 mL ethyl acetate. The organic phase was washed with water, dried and evaporated down in vacuo. Precipitated crystals were filtered off and washed with ether. 3 g of a compound 8 were obtained which was used for the next reaction without further purification.

0.6 g of compound 8 were dissolved in 5 mL formic acid and refluxed for 15 minutes. Then the solution was evaporated down in vacuo and the residue was combined with ethyl acetate and petroleum ether, the precipitate was filtered off and the mother liquor was evaporated down. This yielded 0.58 g of a yellow oily product 7 which was used for the subsequent reactions without further purification.

EXAMPLE 6

0.1 g of 7 was heated to 160° C. with 0.14 g 4-amino-N-cyclopropylbenzamide without solvent for 45 minutes. After cooling the reaction mixture was dissolved in dichloromethane and methanol and fractionated on silica gel. Suitable fractions were combined and evaporated down in vacuo. The residue was dissolved in ethyl acetate, combined with oxalate solution from isopropanol, diethyl ether and petroleum ether and the precipitate formed was filtered off and dried. 30 mg of a white solid were obtained.

EXAMPLE 8

0.46 g of 7 was stirred with 0.32 g 4-amino-3-methoxybenzoic acid and 0.32 g p-toluenesulphonic acid in 10 mL dioxane at reflux temperature for 48 h. The reaction mixture was evaporated down and fractionated on silica gel. Suitable fractions were combined and evaporated down in vacuo. The residue was combined with a little ethyl acetate and petroleum ether, the resulting precipitate was filtered off and dried. 0.3 g of the acid 9 were obtained as a beige solid which was used for subsequent reactions without any additional purification.

0.065 g of 9 together with 0.047 g TBTU, 0.2 mL ethyldiisopropylamine in 2 mL dichloromethane was combined with trans-4-morpholino-cyclohexylamine 10 and stirred for 14 hours at 25° C. Then the mixture was diluted with more dichloromethane and the organic phase was extracted with water and potassium carbonate solution. Then the organic phase was evaporated down and the residue was fractionated by chromatography on silica gel. Suitable fractions were evaporated down and the residue was crystallised by the addition of ethyl acetate and petroleum ether. 50 mg of a white solid were obtained.

The compounds of general formula (I) listed in Table 1, inter alia, are obtained analogously to the procedures described above.

TABLE 1

Ex-	Config.
ample	R1/R2	R¹	R²	R³	R⁴	molecular weight	ESI, [M + H]	melting point

1	R	H	422.53	423

2	R	H	473.58	474

3	R	H	382.47	383

4	R	H	473.58	474

5	R	H	459.55	460

6	R	H	434.54	435

7	R	H	521.66	522

8	R	H	591.75	592	154° C.

9	R	H	612.78	613	118° C.

10	R	H	598.75	599	173° C.

*binding site

As has been found, the compounds of general formula (I) are characterised by their wide range of applications in the therapeutic field. Particular mention should be made of those applications in which the inhibition of specific cell cycle kinases, particularly the inhibiting effect on the proliferation of cultivated human tumour cells but also the proliferation of other cells, such as endothelial cells, for example, plays a part.

As could be demonstrated by DNA staining followed by FACS analysis, the inhibition of proliferation brought about by the compounds according to the invention is mediated by the arrest of the cells, particularly at the G2/M phase of the cell cycle. The cells arrest, depending on the cells used, for a specific length of time in this phase of the cell cycle before programmed cell death is initiated. An arrest in the G2/M phase of the cell cycle is triggered, for example, by the inhibition of specific cell cycle kinases. In view of their biological properties the compounds of general formula I according to the invention, their isomers and their physiologically acceptable salts are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation.

Such diseases include, for example: viral infections (e.g. HIV and Kaposi's sarcoma); inflammatory and autoimmune diseases (e.g. colitis, arthritis, Alzheimer's disease, glomerulonephritis and wound healing); bacterial, fungal and/or parasitic infections; leukaemias, lymphoma and solid tumours; skin diseases (e.g. psoriasis); bone diseases; cardiovascular diseases (e.g. restenosis and hypertrophy). They are also suitable for protecting proliferating cells (e.g. hair, intestinal, blood and progenitor cells) from damage to their DNA caused by radiation, UV treatment and/or cytostatic treatment (Davis et al., 2001).

The new compounds may be used for the prevention, short-term or long-term treatment of the abovementioned diseases, also in combination with other active substances used for the same indications, e.g. cytostatics, hormones or antibodies.

The activity of the compounds according to the invention was determined in the PLK1 inhibition assay, in the cytotoxicity test on cultivated human tumour cells and/or in a FACS analysis, for example on HeLaS3 cells. In both test methods, the compounds exhibited a good to very good activity, i.e. for example an EC₅₀value in the HeLaS3 cytotoxicity test of less than 5 μmol/L, generally less than 1 μmol/L and an IC₅₀value in the PLK1 inhibition assay of less than 1 μmol/L.

PLK1 Kinase Assay

Preparation of Enzyme:

Recombinant human PLK1 enzyme attached to GST at its N-terminal end is isolated from Baculovirus-infected insect cells (Sf21). Purification is carried out by affinity chromatography on glutathione sepharose columns.

4×10⁷Sf21 cells (Spodoptera frugiperda) in 200 ml of Sf-900 II Serum free insect cell medium (Life Technologies) are seeded in a spinner flask. After 72 hours' incubation at 27° C. and 70 rpm, 1×10⁸Sf21 cells are seeded in a total of 180 ml medium in a new spinner flask. After another 24 hours, 20 ml of recombinant Baculovirus stock suspension are added and the cells are cultivated for 72 hours at 27° C. at 70 rpm. 3 hours before harvesting, okadaic acid is added (Calbiochem, final concentration 0.1 μM) and the suspension is incubated further. The cell number is determined, the cells are removed by centrifuging (5 minutes, 4° C., 800 rpm) and washed 1× with PBS (8 g NaCl/I, 0.2 g KCl/I, 1.44 g Na₂HPO₄/I, 0.24 g KH₂PO₄/I). After centrifuging again the pellet is flash-frozen in liquid nitrogen. Then the pellet is quickly thawed and resuspended in ice-cold lysing buffer (50 mM HEPES pH 7.5, 10 mM MgCl₂, 1 mM DTT, 5 μg/ml leupeptin, 5 μg/ml aprotinin, 100 μM NaF, 100 μM PMSF, 10 mM β-glycerolphosphate, 0.1 mM Na₃VO₄, 30 mM 4-nitrophenylphosphate) to give 1×10⁸cells/17.5 ml. The cells are lysed for 30 minutes on ice. After removal of the cell debris by centrifugation (4000 rpm, 5 minutes) the clear supernatant is combined with glutathione sepharose beads (1 ml resuspended and washed beads per 50 ml of supernatant) and the mixture is incubated for 30 minutes at 4° C. on a rotating board. Then the beads are washed with lysing buffer and the recombinant protein is eluted from the beads with 1 ml eluting buffer/ml resuspended beads (eluting buffer: 100 mM Tris/HCl pH=8.0, 120 mM NaCl, 20 mM reduced glutathione (Sigma G-4251), 10 mM MgCl₂, 1 mM DTT). The protein concentration is determined by Bradford Assay.

Assay

The following components are combined in a well of a 96-well round-bottomed dish (Greiner bio-one, PS Microtitre plate No. 650101):

- 10 μl of the compound to be tested in variable concentrations (e.g. beginning at 300 μM, and dilution to 1:3) in 6% DMSO, 0.5 mg/ml casein (Sigma C-5890), 60 mM β-glycerophosphate, 25 mM MOPS pH=7.0, 5 mM EGTA, 15 mM MgCl₂, 1 mM DTT
- 20 μl substrate solution (25 mM MOPS pH=7.0, 15 mM MgCl₂, 1 mM DTT, 2.5 mM EGTA, 30 mM β-glycerophosphate, 0.25 mg/ml casein)
- 20 μl enzyme dilution (1:100 dilution of the enzyme stock in 25 mM MOPS pH=7.0, 15 mM MgCl₂, 1 mM DTT)
- 10 μl ATP solution (45 μM ATP with 1.11×10⁶Bq/ml gamma-P33-ATP).

The reaction is started by adding the ATP solution and continued for 45 minutes at 30° C. with gentle shaking (650 rpm on an IKA Schüttler MTS2). The reaction is stopped by the addition of 125 μl of ice-cold 5% TCA per well and incubated on ice for at least 30 minutes. The precipitate is transferred by harvesting onto filter plates (96-well microtitre filter plate: UniFilter-96, GF/B; Packard; No. 6005177), then washed four times with 1% TCA and dried at 60° C. After the addition of 35 μl scintillation solution (Ready-Safe; Beckmann) per well the plate is sealed shut with sealing tape and the amount of P33 precipitated is measured with the Wallac Betacounter.

The measured data are evaluated using the standard Graphpad software (Levenburg-Marquard Algorhythmus).

Measurement of Cytotoxicity on Cultivated Human Tumour Cells

To measure cytotoxicity on cultivated human tumour cells, cells of cervical carcinoma tumour cell line HeLa S3 (obtained from American Type Culture Collection (ATCC)) are cultivated in Ham's F12 Medium (Life Technologies) and 10% foetal calf serum (Life Technologies) and harvested in the log growth phase. Then the HeLa S3 cells are placed in 96-well plates (Costar) at a density of 1000 cells per well and incubated overnight in an incubator (at 37° C. and 5% CO2), while on each plate 6 wells are filled with medium alone (3 wells as the medium control, 3 wells for incubation with reduced AlamarBlue reagent). The active substances are added to the cells in various concentrations (dissolved in DMSO; DMSO final concentration: 0.1%) (in each case as a triple measurement). After 72 hours incubation 20 μl AlamarBlue reagent (AccuMed International) are added to each well, and the cells are incubated for a further 7 hours. As a control, 20 μl reduced AlamarBlue reagent is added to each of 3 wells (AlamarBlue reagent, which is autoclaved for 30 min). After 7 h incubation the colour change of the AlamarBlue reagent in the individual wells is determined in a Perkin Elmer fluorescence spectrophotometer (excitation 530 nm, emission 590 nm, slits 15, integrate time 0.1). The amount of AlamarBlue reagent reacted represents the metabolic activity of the cells. The relative cell activity is calculated as a percentage of the control (HeLa S3 cells without inhibitor) and the active substance concentration which inhibits the cell activity by 50% (IC₅₀) is derived. The values are calculated from the average of three individual measurements—with correction of the dummy value (medium control).

FACS Analysis

Propidium iodide (PI) binds stoichiometrically to double-stranded DNA, and is thus suitable for determining the proportion of cells in the G1, S, and G2/M phase of the cell cycle on the basis of the cellular DNA content. Cells in the G0 and G1 phase have a diploid DNA content (2N), whereas cells in the G2 or mitosis phase have a 4N DNA content.

For PI staining, for example, 0.4 million HeLa S3 cells were seeded onto a 75 cm²cell culture flask, and after 24 h either 0.1% DMSO was added as control or the substance was added in various concentrations (in 0.1% DMSO). The cells were incubated for 24 h with the substance or with DMSO before the cells were washed 2× with PBS and then detached with trypsin/EDTA. The cells were centrifuged (1000 rpm, 5 min, 4° C.), and the cell pellet was washed 2× with PBS before the cells were resuspended in 0.1 ml PBS. Then the cells were fixed with 80% ethanol for 16 hours at 4° C. or alternatively for 2 hours at −20° C. The fixed cells were centrifuged (1000 rpm, 5 min, 4° C.), washed with PBS and then centrifuged again. The cell pellet was resuspended in 2 ml 0.25% Triton X-100 in PBS, and incubated on ice for 5 min before 5 ml PBS are added and the mixture is centrifuged again. The cell pellet was resuspended in 350 μl PI staining solution (0.1 mg/ml RNase A (Sigma, No. R-4875), 10 μg/ml prodium iodide (Sigma, No. P-4864) in 1×PBS). The cells were incubated for 20 min in the dark with the staining buffer before being transferred into sample measuring containers for the FACS scan. The DNA measurement was carried out in a Becton Dickinson FACS Analyzer, with an argon laser (500 mW, emission 488 nm), and the DNA Cell Quest Programme (BD). The logarithmic Pi fluorescence was determined with a band-pass filter (BP 585/42). The cell populations in the individual cell cycle phases were quantified using the ModFit LT Programme made by Becton Dickinson.

The compounds according to the invention were also tested accordingly on other tumour cells. For example, these compounds are effective on carcinomas of all kinds of tissue (e.g. breast (MCF7); colon (HCT116), head and neck (FaDu), lung (NCI-H460), pancreas (BxPC-3), prostate (DU145)), sarcomas (e.g. SK-UT-1 B, Saos-2), leukaemias and lymphomas (e.g. HL-60, Jurkat, THP-1) and other tumours (e.g. melanomas (BRO), gliomas (U-87MG)) and could be used for such indications. This is evidence of the broad applicability of the compounds according to the invention for the treatment of all kinds of tumour types.

The compounds of general formula (I) may be used on their own or in conjunction with other active substances according to the invention, optionally also in conjunction with other pharmacologically active substances. Suitable preparations include for example tablets, capsules, suppositories, solutions, —particularly solutions for injection (s.c., i.v., i.m.) and infusion—elixirs, emulsions or dispersible powders. The content of the pharmaceutically active compound(s) should be in the range from 0.1 to 90 wt.-%, preferably 0.5 to 50 wt.-% of the composition as a whole, i.e. in amounts which are sufficient to achieve the dosage range specified below. The doses specified may, if necessary, be given several times a day.

Suitable tablets may be obtained, for example, by mixing the active substance(s) with known excipients, for example inert diluents such as calcium carbonate, calcium phosphate or lactose, disintegrants such as corn starch or alginic acid, binders such as starch or gelatine, lubricants such as magnesium stearate or talc and/or agents for delaying release, such as carboxymethyl cellulose, cellulose acetate phthalate, or polyvinyl acetate. The tablets may also comprise several layers.

Coated tablets may be prepared accordingly by coating cores produced analogously to the tablets with substances normally used for tablet coatings, for example collidone or shellac, gum arabic, talc, titanium dioxide or sugar. To achieve delayed release or prevent incompatibilities the core may also consist of a number of layers. Similarly the tablet coating may consist of a number or layers to achieve delayed release, possibly using the excipients mentioned above for the tablets.

Syrups or elixirs containing the active substances or combinations thereof according to the invention may additionally contain a sweetener such as saccharine, cyclamate, glycerol or sugar and a flavour enhancer, e.g. a flavouring such as vanillin or orange extract. They may also contain suspension adjuvants or thickeners such as sodium carboxymethyl cellulose, wetting agents such as, for example, condensation products of fatty alcohols with ethylene oxide, or preservatives such as p-hydroxybenzoates.

Solutions for injection and infusion are prepared in the usual way, e.g. with the addition of isotonic agents, preservatives such as p-hydroxybenzoates, or stabilisers such as alkali metal salts of ethylenediamine tetraacetic acid, optionally using emulsifiers and/or dispersants, whilst if water is used as the diluent, for example, organic solvents may optionally be used as solvating agents or dissolving aids, and transferred into injection vials or ampoules or infusion bottles.

Capsules containing one or more active substances or combinations of active substances may for example be prepared by mixing the active substances with inert carriers such as lactose or sorbitol and packing them into gelatine capsules.

Suitable suppositories may be made for example by mixing with carriers provided for this purpose, such as neutral fats or polyethyleneglycol or the derivatives thereof.

Excipients which may be used include, for example, water, pharmaceutically acceptable organic solvents such as paraffins (e.g. petroleum fractions), vegetable oils (e.g. groundnut or sesame oil), mono- or polyfunctional alcohols (e.g. ethanol or glycerol), carriers such as e.g. natural mineral powders (e.g. kaolins, clays, talc, chalk), synthetic mineral powders (e.g. highly dispersed silicic acid and silicates), sugars (e.g. cane sugar, lactose and glucose) emulsifiers (e.g. lignin, spent sulphite liquors, methylcellulose, starch and polyvinylpyrrolidone) and lubricants (e.g. magnesium stearate, talc, stearic acid and sodium lauryl sulphate).

The preparations are administered by the usual methods, preferably by oral or transdermal route, most preferably by oral route. For oral administration the tablets may, of course contain, apart from the abovementioned carriers, additives such as sodium citrate, calcium carbonate and dicalcium phosphate together with various additives such as starch, preferably potato starch, gelatine and the like. Moreover, lubricants such as magnesium stearate, sodium lauryl sulphate and talc may be used at the same time for the tabletting process. In the case of aqueous suspensions the active substances may be combined with various flavour enhancers or colourings in addition to the excipients mentioned above.

For parenteral use, solutions of the active substances with suitable liquid carriers may be used.

The dosage for intravenous use is from 1-1000 mg per hour, preferably between 5 and 500 mg per hour.

However, it may sometimes be necessary to depart from the amounts specified, depending on the body weight, the route of administration, the individual response to the drug, the nature of its formulation and the time or interval over which the drug is administered. Thus, in some cases it may be sufficient to use less than the minimum dose given above, whereas in other cases the upper limit may have to be exceeded. When administering large amounts it may be advisable to divide them up into a number of smaller doses spread over the day.

The formulation examples which follow illustrate the present invention without restricting its scope:

EXAMPLES OF PHARMACEUTICAL FORMULATIONS


	A) Tablets	per tablet

active substance	100	mg
lactose	140	mg
corn starch	240	mg
polyvinylpyrrolidone	15	mg
magnesium stearate	5	mg
	500	mg

The finely ground active substance, lactose and some of the corn starch are mixed together. The mixture is screened, then moistened with a solution of polyvinylpyrrolidone in water, kneaded, wet-granulated and dried. The granules, the remaining corn starch and the magnesium stearate are screened and mixed together. The mixture is compressed to produce tablets of suitable shape and size.


	B) Tablets	per tablet

active substance	80	mg
lactose	55	mg
corn starch	190	mg
microcrystalline cellulose	35	mg
polyvinylpyrrolidone	15	mg
sodium-carboxymethyl starch	23	mg
magnesium stearate	2	mg
	400	mg

The finely ground active substance, some of the corn starch, lactose, microcrystalline cellulose and polyvinylpyrrolidone are mixed together, the mixture is screened and worked with the remaining corn starch and water to form a granulate which is dried and screened. The sodiumcarboxymethyl starch and the magnesium stearate are added and mixed in and the mixture is compressed to form tablets of a suitable size.


	C) Ampoule solution

active substance	50	mg
sodium chloride	50	mg
water for inj.	5	ml

The active substance is dissolved in water at its own pH or optionally at pH 5.5 to 6.5 and sodium chloride is added to make it isotonic. The solution obtained is filtered free from pyrogens and the filtrate is transferred under aseptic conditions into ampoules which are then sterilised and sealed by fusion. The ampoules contain 5 mg, 25 mg and 50 mg of active substance.

Claims

1. A compound of the formula (I),

wherein

R¹, R²which may be identical or different denote a group selected from among optionally substituted C₁-C₁₀-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, aryl, heteroaryl, C₃-C₈-cycloalkyl, C₃-C₈-heterocycloalkyl, —X-aryl, —X-heteroaryl, —X-cycloalkyl, —X-heterocycloalkyl, —NR⁷-aryl, —NR⁷-heteroaryl, —NR⁷-cycloalkyl and —NR⁷-heterocycloalkyl,

or

a group selected from among hydrogen, halogen, COXR⁷, CON(R⁷)₂, COR⁷and XR⁷,

or

R¹and R²together denote a 2- to 5-membered alkyl bridge which may contain 1 to 2 heteroatoms,

R³denotes hydrogen or a group selected from among optionally substituted C₁-C₁₂-alkyl, C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl, aryl, heteroaryl, —C₃-C₁₂-cycloalkyl, C₃-C₁₂-cycloalkenyl, C₇-C₁₂-polycycloalkyl, C₇-C₁₂-polycycloalkenyl and C₅-C₁₂-spirocycloalkyl or

R¹and R³or R²and R³together denote a saturated or unsaturated C₃-C₄-alkyl bridge which may contain 1 to 2 heteroatoms,

R⁴denotes optionally substituted aryl, benzyl or heteroaryl,

R⁵denotes hydrogen, —CO—NH—C₁-C₄-alkyl, —CO—C₁-C₄-alkyl or —CO—X—C₁-C₄-alkyl,

R⁶denotes a group selected from among hydrogen, NH₂, XH, halogen and a C₁-C₃-alkyl group optionally substituted by one or more halogen atoms,

and

R⁷each independently of one another denote hydrogen or a group selected from among optionally substituted C₁-C₄-alkyl, C₂-C₄-alkenyl, C₂-C₄-alkynyl, benzyl and phenyl,

X denotes O or S,

optionally in the form of the tautomers, racemates, enantiomers, diastereomers and mixtures thereof, and optionally the pharmacologically acceptable acid addition salts, thereof.

2. The compound according to claim 1,

wherein

R⁵and R⁶represent hydrogen.

3. The compound according to claim 2,

wherein

R¹, R²which may be identical or different denote hydrogen or a group selected from among optionally substituted C₁-C₆-alkyl, C₂-C₆-alkenyl, and C₂-C₆-alkynyl,

or

R¹and R²together denote a 2- to 5-membered alkyl bridge.

4. The compound according to claim 3,

wherein

R³is hydrogen or a group selected from among optionally substituted C₁-C₁₂-alkyl, C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl and C₆-C₁₄-aryl, or a group selected from among optionally substituted C₃-C₁₂-cycloalkyl, C₃-C₁₂-cycloalkenyl, C₇-C₁₂-polycycloalkyl, C₇-C₁₂-polycycloalkenyl and C₅-C₁₂-spirocycloalkyl.

5. The compound according to claim 4,

wherein

R⁴denotes a group of the formula

R⁸which may be identical or different denote hydrogen or a group selected from among optionally substituted C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, —O—C₁-C₆-alkyl, —O—C₂-C₆-alkenyl, —O—C₂-C₆-alkynyl, heterocycloalkyl, C₃-C₆-cycloalkyl, aryl, heteroaryl, —O-aryl, —O-heteroaryl, —O-cycloalkyl, and —O-heterocycloalkyl or

a group selected from among hydrogen, —CONH₂, —COOR⁷, —OCON(R⁷)₂, —N(R⁷)₂, —NHCOR⁷, —NHCON(R⁷)₂, —NO₂, CF₃, halogen, —O—C₁-C₆-alkyl-Q¹, —CONR⁷—C₁-C₁₀-alkyl-Q¹, —CONR⁷—C₁-C₁₀-alkenyl-Q¹, —CONR⁷-Q², halogen, OH, —SO₂R⁷, —SO₂N(R⁷)₂, —COR⁷, —COOR⁷, —N(R⁷)₂, —NHCOR⁷, —CONR⁷OC₁-C₁₀-alkyl-Q¹and CONR⁷O—Q²,

or

adjacent groups R⁸together denote a bridge of the formula a), b), c) or d),

Y denotes O, S or NR¹¹,

m denotes 0, 1 or 2

R⁹denotes C₁-C₆-alkyl

R¹⁰denotes hydrogen or a group selected from among optionally substituted phenyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, piperidinyl, piperazinyl, —C₁-C₃-alkyl-phenyl, —C₁-C₃-alkyl-pyridyl, —C₁-C₃-alkyl-pyrazinyl, —C₁-C₃-alkyl-pyrimidinyl and —C₁-C₃-alkyl-pyridazinyl,

R¹¹denotes hydrogen or C¹-C⁴-alkyl

Q¹denotes hydrogen, —NHCOR⁷, or a group selected from among an optionally substituted —NH-aryl, —NH-heteroaryl, aryl, heteroaryl, C₃-C₈-cycloalkyl and heterocycloalkyl group,

Q²denotes hydrogen or a group selected from among an optionally substituted aryl, heteroaryl, C₃-C₈-heterocycloalkyl, C₃-C₈-cycloalkyl and C₁-C₄-alkyl-C₃-C₈-cycloalkyl group,

and

n denotes 0, 1, 2, 3, 4 or 5.

6. The compound according to claim 5,

wherein

R¹, R²which may be identical or different denote hydrogen or a group selected from among methyl, ethyl, propyl, allyl and propargyl

or

R¹and R²together represent cyclopropyl,

R³is hydrogen, or denotes optionally substituted C₁-C₆-alkyl or optionally substituted C₃-C₁₂-cycloalkyl.

7. The compound according to claim 5 or 6,

wherein

R⁸which may be identical or different denote hydrogen or a group selected from among halogen, (C₁-C₂-alkyl)₂N, CF₃, NH₂SO₂, —CONH—C₆-C₁₄-aryl, —CONH—C₁-C₄-alkyl-C₆-C₁₄-aryl, —CONH—C₁-C₄-alkyl-C₆-C₁₄-heteroaryl, —CONH—C₃-C₈-cycloalkyl-heterocycloalkyl and —O—C₁-C₄-alkyl.

8. A pharmaceutical composition comprising a pharmaceutically effective amount of a compound according to claim 1 optionally combined with conventional excipients and/or carriers.